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Lisinopril and Hydrochlorothiazide - 63629-1679-1 - (Lisinopril and Hydrochlorothiazide)

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Drug Information of Lisinopril and Hydrochlorothiazide

Product NDC: 63629-1679
Proprietary Name: Lisinopril and Hydrochlorothiazide
Non Proprietary Name: Lisinopril and Hydrochlorothiazide
Active Ingredient(s): 12.5; 10    mg/1; mg/1 & nbsp;   Lisinopril and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril and Hydrochlorothiazide

Product NDC: 63629-1679
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075776
Marketing Category: ANDA
Start Marketing Date: 20020701

Package Information of Lisinopril and Hydrochlorothiazide

Package NDC: 63629-1679-1
Package Description: 90 TABLET in 1 BOTTLE (63629-1679-1)

NDC Information of Lisinopril and Hydrochlorothiazide

NDC Code 63629-1679-1
Proprietary Name Lisinopril and Hydrochlorothiazide
Package Description 90 TABLET in 1 BOTTLE (63629-1679-1)
Product NDC 63629-1679
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020701
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name HYDROCHLOROTHIAZIDE; LISINOPRIL
Strength Number 12.5; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Lisinopril and Hydrochlorothiazide


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